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携带来自半抗原化表皮细胞分子的脂质体诱导和抑制接触敏感性

Induction and suppression of contact sensitivity by liposomes carrying molecules from haptenated epidermal cells.

作者信息

Yokozeki H, Nishioka K, Katayama I, Takijiri C, Hashimoto K

出版信息

J Invest Dermatol. 1985 Jan;84(1):33-6. doi: 10.1111/1523-1747.ep12274625.

Abstract

Liposomes carrying molecules from trinitrophenylated epidermal cells (TNP-EC) liposomes stimulated the hapten-specific proliferation of lymphocytes in vitro in our previous study. In order to analyze the role of TNP-EC liposomes in vivo, they were injected into naive mice. TNP-EC liposomes induced contact sensitivity effectively when injected either s.c. or i.p. Contact sensitivity induced by TNP-EC liposomes was a long-lived T cell-mediated reaction. A s.c. injection of liposomes with molecules from TNP-Ia antigen-depleted epidermal cells [TNP-EC (Ia-) liposomes] failed to induce contact sensitivity and developed unresponsiveness. This unresponsiveness was transferred by T cells, i.e., suppressor T cells. Therefore, it is suggested that Ia antigens in epidermal cells play a critical role for induction and suppression of contact sensitivity.

摘要

在我们之前的研究中,携带来自三硝基苯基化表皮细胞(TNP-EC)脂质体分子的脂质体在体外刺激了淋巴细胞的半抗原特异性增殖。为了分析TNP-EC脂质体在体内的作用,将它们注射到未接触过抗原的小鼠体内。当经皮下或腹腔注射时,TNP-EC脂质体可有效诱导接触性敏感。TNP-EC脂质体诱导的接触性敏感是一种持久的T细胞介导反应。皮下注射含有来自TNP-Ia抗原缺失表皮细胞的分子的脂质体[TNP-EC(Ia-)脂质体]未能诱导接触性敏感,反而产生了无反应性。这种无反应性由T细胞即抑制性T细胞传递。因此,提示表皮细胞中的Ia抗原在接触性敏感的诱导和抑制中起关键作用。

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